Evidence map›Paper›PMID 25751158›Full record

ArticleCell transplantation2016

Preconditioning of Cardiosphere-Derived Cells With Hypoxia or Prolyl-4-Hydroxylase Inhibitors Increases Stemness and Decreases Reliance on Oxidative Metabolism.

Suat Cheng Tan, Renata S M Gomes, Kar Kheng Yeoh, Filippo Perbellini, Sophia Malandraki-Miller, Lucy Ambrose, Lisa C Heather, Giuseppe Faggian, Christopher J Schofield, Kay E Davies and 2 more

Open access · greenAbstract read
In one paragraph

Article in Cell transplantation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Pooled it
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  18. Eat, breathe, ROS: controlling stem cell fate through metabolism.Expert review of cardiovascular therapy · 2017
    Review
  19. Article
  20. Comparing theJournal of stem cells & regenerative medicine · 2017
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 3 countries.

Suat Cheng TanDepartment of Physiology, Anatomy and Genetics, University of Oxford, Oxford, UK.
Renata S M Gomes
Kar Kheng Yeoh
Filippo Perbellini
Sophia Malandraki-Miller
Lucy Ambrose
Lisa C Heather
Giuseppe Faggian
Christopher J Schofield
Kay E Davies
Kieran Clarke
Carolyn A Carr
University of Oxford · GBUniversity of Verona · ITUniversiti Sains Malaysia · MY

Funding

Biotechnology and Biological Sciences Research Council BB/D011523/1Biotechnology and Biological Sciences Research Council BB/L009846/1British Heart Foundation PG/07/059/23259British Heart Foundation PG/12/33/29546British Heart Foundation PG/13/34/30216Cancer Research UK 16466Diabetes UK 11/0004175Wellcome Trust 084655
6 · The paper itself

Abstract

Cardiosphere-derived cells (CDCs), which can be isolated from heart explants, are a promising candidate cell source for infarcted myocardium regeneration. However, current protocols used to expand CDCs require at least 1 month in vitro to obtain sufficient cells for transplantation. We report that CDC culture can be optimized by preconditioning the cells under hypoxia (2% oxygen), which may reflect the physiological oxygen level of the stem cell niche. Under hypoxia, the CDC proliferation rate increased by 1.4-fold, generating 6 × 10(6) CDCs with higher expression of cardiac stem cell and pluripotency gene markers compared to normoxia. Furthermore, telomerase (TERT), cytokines/ligands involved in stem cell trafficking (SDF/CXCR-4), erythropoiesis (EPO), and angiogenesis (VEGF) were increased under hypoxia. Hypoxic preconditioning was mimicked by treatment with two types of hypoxia-inducible factor (HIF) prolyl-4-hydroxylase inhibitors (PHDIs): dimethyloxaloylglycine (DMOG) and 2-(1-chloro-4-hydroxyisoquinoline-3-carboxamido) acetic acid (BIC). Despite the difference in specificity, both PHDIs significantly increased c-Kit expression and activated HIF, EPO, and CXCR-4. Furthermore, treatment with PHDIs for 24 h increased cell proliferation. Notably, all hypoxic and PHDI-preconditioned CDCs had decreased oxygen consumption and increased glycolytic metabolism. In conclusion, cells cultured under hypoxia could have potentially enhanced therapeutic potential, which can be mimicked, in part, by PHDIs.

Indexed as

AnimalsBiomarkersCell DifferentiationCell HypoxiaCell ProliferationFemaleGene Expression RegulationGlucoseHypoxia-Inducible Factor 1, alpha SubunitMyocardiumOxidation-ReductionProlyl-Hydroxylase InhibitorsProlyl HydroxylasesRats, Sprague-DawleyRNA, MessengerSpheroids, CellularBiomarkersGlucoseHypoxia-Inducible Factor 1, alpha SubunitProlyl-Hydroxylase InhibitorsProlyl HydroxylasesRNA, Messenger

Identifiers

PMID25751158
PMCPMC6042641
OpenAlexW197652504

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.